v1
Imprinting mutation in the Beckwith-Wiedemann syndrome leads to biallelic IGF2 expression through an H19-independent pathway.
Identifier:nobleid.org/w1/20260515/F721DF59
Type:Journal Article
0 views
Embeddable Badge
[](https://nobleid.org/work/w1/20260515/F721DF59)
Bibliometric Analysis
Impact metrics, research fronts, co-authorship networks →
Authors & Claims